2 3 Methyl 4 2 2 2 Trifluoroethoxy Pyridin 2 Yl Methyl Sulfanyl 1h Benzimidazole
quinoline thiophene imidazole thiazole

2-({[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methyl}sulfanyl)-1H-benzimidazole

    Specifications

    HS Code

    662957

    Chemical Formula C18H16F3N3OS
    Molecular Weight 381.4 g/mol
    Appearance Solid (predicted)
    Solubility In Water Low (predicted)
    Logp Predicted value indicating lipophilic nature
    Pka Predicted values for acidic or basic groups (if applicable)
    Vapor Pressure Very low (predicted)
    Stability Stable under normal conditions (predicted)

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    Frequently Asked Questions

    As a leading 2-({[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methyl}sulfanyl)-1H-benzimidazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 2- ({[3-methyl-4- (2,2,2-trifluoroethoxy) pyridin-2-yl] methyl} sulfanyl) -1H-benzimidazole?
    Alas! This is the question of the structure of chemical substances. 2 - {[3-methyl-4 - (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thioalkyl-1H-benzimidazole, its chemical structure is analyzed as follows.
    First look at the nucleus of benzimidazole, which is a nitrogen-containing fused ring structure, which is formed by fusing the benzene ring with the imidazole ring. 1H-benzimidazole has a hydrogen atom at the 1 position.
    Looking at the side chain again, there is a complex group connected at the 2 positions. In this group, {[3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thioalkyl. Among them, the pyridine ring is a six-membered nitrogen-containing heterocycle with methyl substitution at the 3rd position and 2,2,2-trifluoroethoxy at the 4th position. The 2nd position of the pyridine ring is connected to a methylene group, which is in turn connected to the sulfur atom, and the sulfur atom is further connected to the 2nd position of benzimidazole.
    In this structure, the nitrogen atom of benzimidazole has a lone pair electron, which can participate in chemical reactions and coordination. The substituents on the pyridine ring, such as methyl, can affect the spatial structure and electron cloud distribution of the molecule. The strong electron-absorbing fluorine atom of trifluoroethoxy can change the electronic properties of the pyridine ring and the whole molecule, and affect the chemical activity, solubility and stability of the molecule. The presence of thioalkyl groups also gives the molecule specific chemical properties and reactivity. In this way, the chemical structure of 2 - {[3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thioalkyl-1H-benzimidazole is formed.
    What are the main uses of 2- ({[3-methyl-4- (2,2,2-trifluoroethoxy) pyridin-2-yl] methyl} sulfanyl) -1H-benzimidazole?
    2 - {[3-methyl-4 - (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thio-1H-benzimidazole, this compound has a wide range of uses. In the field of medicine, it can be used as a pharmaceutical active ingredient, interacting with targets in vivo through specific chemical structures, or participating in the treatment process of diseases. For some specific diseases, it may be able to precisely act on pathogenic-related proteins, enzymes or receptors, and then play a role in regulating physiological functions and alleviating diseases.
    In the field of pesticides, it may have insecticidal, bactericidal or herbicidal properties. If used for insecticides, it can interfere with the normal physiological activities of the nervous system and respiratory system of pests by means of unique chemical properties, causing the death of pests, achieving the purpose of controlling pests and protecting crops; when used as fungicides, it may inhibit the growth and reproduction of pathogenic bacteria, prevent crops from being infested by diseases, and ensure crop yield and quality.
    In the field of materials science, or due to special chemical structures and properties, it can be used to prepare materials with special properties. If properly modified and processed, or materials with selective adsorption and separation functions for specific substances can be prepared, which can be used in the separation and purification of substances in chemical production, environmental protection and other fields. < Br >
    Or it can be used to prepare materials with special optical and electrical properties, providing new material options for the development of electronic devices, optical equipment and other fields to meet the needs of new display materials, sensor materials, etc. In short, 2 - {[3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thio-1H-benzimidazole has important application value in many fields and is of great significance to promote the development of related fields.
    What is the synthesis method of 2- ({[3-methyl-4- (2,2,2-trifluoroethoxy) pyridin-2-yl] methyl} sulfanyl) -1H-benzimidazole?
    To prepare 2 - {[3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thio-1H-benzimidazole, the method is as follows:
    First take 3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-formaldehyde, and combine it with thiourea in a suitable solvent at a suitable temperature and reaction time to carry out a condensation reaction to obtain the corresponding intermediate. In this step, attention should be paid to the choice of solvent. Those with good solubility of the reactants and no excessive interaction with the reactants should be selected. The temperature and time should also be precisely controlled. If the temperature is too high or too long, the side reactions may occur, and if it is too low, the reaction will be incomplete.
    Then make the above intermediate with an appropriate halogen, such as halogenated methyl benzimidazole, in the presence of a base, in a suitable solvent, carry out nucleophilic substitution reaction. The strength and dosage of the base should be carefully considered. If the base is too strong or too much dosage, it may cause side reactions such as the elimination of the halogen. The solvent should also be able to dissolve the reactants and facilitate the reaction. < Br >
    After the reaction is completed, the product is purified by conventional separation and purification methods, such as column chromatography, recrystallization, etc. During column chromatography, the appropriate eluent system is selected to effectively separate impurities and products. Recrystallization requires the selection of a suitable solvent to dissolve the product in a hot solvent, and crystallize and precipitate after cooling, while the impurities are left in the mother liquor to obtain a pure 2- {[3-methyl-4- (2,2,2-trifluoroethoxy) pyridine-2-yl] methyl} thio-1H-benzimidazole.
    What are the physical properties of 2- ({[3-methyl-4- (2,2,2-trifluoroethoxy) pyridin-2-yl] methyl} sulfanyl) -1H-benzimidazole?
    2-%28+%7B%5B3-methyl-4-%282%2C2%2C2-trifluoroethoxy%29pyridin-2-yl%5Dmethyl%7Dsulfanyl%29-1H-benzimidazole is an organic compound with unique physical properties. Its appearance is often white to light yellow crystalline powder, which is easy to identify and observe.
    Discussing solubility, this compound has different solubility in organic solvents. In common organic solvents such as dichloromethane and chloroform, it has a certain solubility and can be well dispersed and dissolved. This property makes it conducive to participating in various reactions in organic synthesis and related experimental operations. However, the solubility in water is low, which is due to the large proportion of organic groups in its molecular structure, resulting in poor hydrophilicity.
    Melting point is also an important physical property. After determination, the melting point of the compound is in a specific range, and the exact value of the melting point is of great significance for the identification of its purity. The melting point of the compound with high purity is relatively fixed. If the melting point of the sample deviates greatly from the theoretical value, it may suggest that its purity is questionable.
    In addition, the stability of the compound is worthy of attention. Under normal storage conditions, in a dry and cool place, it can maintain a relatively stable chemical structure. However, in extreme chemical environments such as strong acids and bases, its structure may change, triggering chemical reactions and resulting in changes in properties. And under specific physical conditions such as light and high temperature, decomposition or deterioration may also occur, so attention should be paid when storing and using.
    What is the market outlook for 2- ({[3-methyl-4- (2,2,2-trifluoroethoxy) pyridin-2-yl] methyl} sulfanyl) -1H-benzimidazole?
    2-%28+%7B%5B3-methyl-4-%282%2C2%2C2-trifluoroethoxy%29pyridin-2-yl%5Dmethyl%7Dsulfanyl%29-1H-benzimidazole, this is a complex organic compound. The analysis of its market prospects needs to be considered from multiple perspectives.
    In the field of medicine, it may have potential medicinal value. If it can be proved to have curative effect on specific diseases, such as antibacterial, antiviral or anti-tumor, it must attract the attention of pharmaceutical companies. The current research and development of innovative drugs is high, and there is a strong demand for compounds with novel structures. If this compound exhibits unique pharmacological activity through research, pharmaceutical companies may invest resources in development, and its market prospect is bright.
    In the chemical industry, or as a synthetic intermediate. Because of its unique chemical structure, a series of high value-added products may be derived. The chemical industry continues to seek new raw materials and intermediates to improve product performance and quality. If this compound can meet the needs of chemical synthesis, or become an important raw material for chemical enterprises, the market demand is considerable.
    However, there are challenges in its market expansion. The synthesis process may be complex, resulting in high production costs and affecting market competitiveness. And the research and development of new drugs requires long and rigorous clinical trials, with great uncertainty. If there are no positive results in pharmacological research, it will be difficult to enter the pharmaceutical market.
    In summary, 2-%28+%7B%5B3-methyl-4-%282%2C2%2C2-trifluoroethoxy%29pyridin-2-yl%5Dmethyl%7Dsulfanyl%29-1H-benzimidazole have addressable market opportunities, it is necessary to overcome problems such as synthesis costs and pharmacological verification in order to emerge in the market.